Canonical Allele Identifier: CA2697393042
Gene:

Linked Data

dbSNP Id: rs2101874755
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649271C>T , CM000663.2:g.168649271C>T GRCh38
NC_000001.10:g.168618509C>T , CM000663.1:g.168618509C>T GRCh37
NC_000001.9:g.166885133C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-7996G>A
XR_922259.2:n.332-7996G>A
Search 100 bp 5'
Search 100 bp 3'